ClinVar Miner

List of variants in gene GRIN2B reported as not provided

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Total variants: 16
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HGVS dbSNP
NM_000834.4(GRIN2B):c.1341C>T (p.Asp447=) rs35025065
NM_000834.4(GRIN2B):c.14C>T (p.Ala5Val) rs367543147
NM_000834.4(GRIN2B):c.15G>A (p.Ala5=) rs34315573
NM_000834.4(GRIN2B):c.1833T>C (p.Gly611=) rs367543148
NM_000834.4(GRIN2B):c.2087G>A (p.Arg696His) rs1555103971
NM_000834.4(GRIN2B):c.2313G>A (p.Gly771=) rs150554184
NM_000834.4(GRIN2B):c.2664C>T (p.Thr888=) rs1806201
NM_000834.4(GRIN2B):c.2691C>T (p.Asn897=) rs35125534
NM_000834.4(GRIN2B):c.2712G>A (p.Thr904=) rs199843136
NM_000834.4(GRIN2B):c.3562G>A (p.Gly1188Ser) rs367543149
NM_000834.4(GRIN2B):c.3648C>T (p.Arg1216=) rs201405157
NM_000834.4(GRIN2B):c.4197T>C (p.His1399=) rs1805247
NM_000834.4(GRIN2B):c.4218C>T (p.Phe1406=) rs1805246
NM_000834.4(GRIN2B):c.4240G>T (p.Ala1414Ser) rs140744818
NM_000834.4(GRIN2B):c.465C>A (p.Ser155=) rs115189840
NM_000834.4(GRIN2B):c.466G>A (p.Val156Ile) rs1555133189

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